Overview
Angela Sitta practices in Porto Alegre, Brazil. Ms. Sitta is rated as an Experienced expert by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Glutaric Acidemia Type 1, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Maple Syrup Urine Disease, and Phenylketonuria (PKU).
Her clinical research consists of co-authoring 38 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Carbamoyl Phosphate Synthetase 1 Deficiency.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Glutaric Acidemia Type 1Ms. Sitta isAdvanced. Learn about Glutaric Acidemia Type 1.
- Maple Syrup Urine DiseaseMs. Sitta isAdvanced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaMs. Sitta isAdvanced. Learn about Methylmalonic Acidemia.
- Orotic Aciduria Type 1Ms. Sitta isAdvanced. Learn about Orotic Aciduria Type 1.
- Phenylketonuria (PKU)Ms. Sitta isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- Argininosuccinic AciduriaMs. Sitta isExperienced. Learn about Argininosuccinic Aciduria.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CitrullinemiaMs. Sitta isExperienced. Learn about Citrullinemia.
- HomocystinuriaMs. Sitta isExperienced. Learn about Homocystinuria.
- Inborn Amino Acid Metabolism DisorderMs. Sitta isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- L-2-Hydroxyglutaric AciduriaMs. Sitta isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.